Canonical Allele Identifier: CA7627112
Community Standard Title: NM_024666.5(AAGAB):c.451+3_451+6del
Gene: AAGAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67235975_67235978del , CM000677.2:g.67235975_67235978del GRCh38
NC_000015.9:g.67528313_67528316del , CM000677.1:g.67528313_67528316del GRCh37
NC_000015.8:g.65315367_65315370del NCBI36
NG_033007.1:g.24223_24226del

Transcript Alleles

HGVS Amino-acid Change
NM_024666.5:c.451+3_451+6del MANE Select NP_078942.3:n.451+3_451+6del
ENST00000261880.10:c.451+3_451+6del MANE Select ENSP00000261880.5:n.451+3_451+6del
NM_001271885.1:c.124+3_124+6del NP_001258814.1:n.124+3_124+6del
NM_001271885.2:c.124+3_124+6del NP_001258814.1:n.124+3_124+6del
NM_001271886.1:c.124+3_124+6del NP_001258815.1:n.124+3_124+6del
NM_001271886.2:c.124+3_124+6del NP_001258815.1:n.124+3_124+6del
NM_024666.4:c.451+3_451+6del NP_078942.3:n.451+3_451+6del
ENST00000261880.9:c.451+3_451+6del ENSP00000261880.5:n.451+3_451+6del
ENST00000542650.5:c.124+3_124+6del ENSP00000440735.1:n.124+3_124+6del
ENST00000558725.5:n.474+3_474+6del
ENST00000560362.1:c.124+3_124+6del ENSP00000453059.1:n.124+3_124+6del
ENST00000561452.5:c.124+3_124+6del ENSP00000453263.1:n.124+3_124+6del
XM_005254664.2:c.451+3_451+6del XP_005254721.1:n.451+3_451+6del
XM_006720683.2:c.451+3_451+6del XP_006720746.1:n.451+3_451+6del
XM_011522020.1:c.124+3_124+6del XP_011520322.1:n.124+3_124+6del
XM_024450052.1:c.451+3_451+6del XP_024305820.1:n.451+3_451+6del
XM_024450053.1:c.451+3_451+6del XP_024305821.1:n.451+3_451+6del